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首页> 外文期刊>Alimentary pharmacology & therapeutics. >High dosage rifaximin for the treatment of small intestinal bacterial overgrowth.
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High dosage rifaximin for the treatment of small intestinal bacterial overgrowth.

机译:大剂量利福昔明用于治疗小肠细菌过度生长。

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Background Rifaximin is a broad spectrum non-absorbable antibiotic used for treatment of small intestinal bacterial overgrowth. Doses of 1200 mg/day showed a decontamination rate of 60% with low side-effects incidence. Aims To assess efficacy, safety and tolerability of rifaximin 1600 mg with respect to 1200 mg/day for small intestinal bacterial overgrowth treatment. Methods Eighty consecutive small intestinal bacterial overgrowth patients were enrolled. Diagnosis of small intestinal bacterial overgrowth based the clinical history and positivity to H(2)/CH(4) glucose breath test. Patients were randomized in two 7-day treatment groups: rifaximin 1600 mg (group 1); rifaximin 1200 mg (group 2). Glucose breath test was reassessed 1 month after. Compliance and side-effect incidence were also evaluated. Results One drop-out was observed in group 1 and two in group 2. Glucose breath test normalization rate was significantly higher in group 1 with respect to group 2 both in intention-to-treat (80% vs. 58%; P <0.05) and per protocol analysis (82% vs. 61%; P < 0.05). No significant differences in patient compliance and incidence of side effects were found between groups. Conclusions Rifaximin 1600 mg/day showed a significantly higher efficacy for small intestinal bacterial overgrowth treatment with respect to 1200 mg with similar compliance and side-effect profile.
机译:背景利福昔明是一种广谱的不可吸收抗生素,用于治疗小肠细菌过度生长。 1200毫克/天的剂量显示去污率为60%,且副作用发生率较低。目的评估小肠细菌过度生长治疗中相对于1200 mg / day的rifaximin 1600 mg的疗效,安全性和耐受性。方法连续入选80例小肠细菌过度生长患者。小肠细菌过度生长的诊断基于临床历史和对H(2)/ CH(4)葡萄糖呼气试验的阳性。将患者随机分为两个7天治疗组:利福昔明1600 mg(第1组);利福昔明1200 mg(第2组)。 1个月后重新评估了葡萄糖呼气试验。还评估了依从性和副作用发生率。结果在第1组中观察到1例退出研究,在第2组中观察到2例退出研究。在意向治疗方面,第1组中的葡萄糖呼气测试正常化率均高于第2组(80%比58%; P <0.05 )和方案分析(82%对61%; P <0.05)。两组之间在患者依从性和副作用发生率方面无显着差异。结论利福昔明1600 mg / day对小肠细菌过度生长治疗的疗效显着高于1200 mg,具有相似的依从性和副作用。

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